Brain Morphological Defects in Prolidase Deficient Mice: First Report

Prolidase gene (PEPD) encodes prolidase enzyme, which is responsible for hydrolysis of dipeptides containing proline or hydroxypro-line at their C-terminal end. Mutations in PEPD gene cause, in human, prolidase deficiency (PD), a rare autosomal recessive disorder. PD patients show reduced or absent...

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Detalles Bibliográficos
Autores principales: Insolia, V., Piccolini, V.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2014
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194396/
https://www.ncbi.nlm.nih.gov/pubmed/25308848
http://dx.doi.org/10.4081/ejh.2014.2417

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194396/
https://www.ncbi.nlm.nih.gov/pubmed/25308848
http://dx.doi.org/10.4081/ejh.2014.2417

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